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NCT01165814 Clinical Trial

Naproxen Versus Tramadol for Post Cesarean Pain Control

Pain Clinical Trial

Official title:
Oral Naproxen Versus Oral Tramadol for Analgesia After Cesarean Delivery - A Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01165814
Other study ID # TRAMNAP
Secondary ID
Status Completed
Phase N/A
First received July 18, 2010
Last updated July 19, 2010
Start date August 2006
Est. completion date March 2009

Study information
Verified date July 2010
Source Bnai Zion Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

Oral naproxen might be more efficacious for post-cesarean pain-control and have better side-effects profile than oral tramadol.

Recruitment information / eligibility
Status Completed
Enrollment 120
Est. completion date March 2009
Est. primary completion date March 2009
Accepts healthy volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- all patients after cesarean section

Exclusion Criteria:

- emergent CS

- hypersensitivity to drug

- drug abuse

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Naproxen Tramadol

Locations
Country Name City State
Israel Bnai Zion Medical Center Haifa

Sponsors (1)
Lead Sponsor Collaborator
Bnai Zion Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain Score
Secondary Side effects
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